Regulatory Affairs Associate II – Hybrid (Class III Devices)

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actalentNorth Chicago (IL)

Regulatory Affairs Managers Electromedical and Electrotherapeutic Apparatus Manufacturing

SENIORITY

Senior

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About the role

Actalent is seeking a Regulatory Affairs Associate II in North Chicago, IL, to lead preparation of regulatory submissions for Class III implantable medical devices and manage ongoing regulatory activities. You will analyze regulatory and technical information, coordinate cross-functional inputs for agency meetings, and ensure compliance across change control, validation, and manufacturing changes, with guidance under limited supervision.

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